RP Cure Tracker

Trials / NCT00447980

A Study of Encapsulated Cell Technology (ECT) Implant for Participants With Early Stage Retinitis Pigmentosa

Completed Phase 2 Drug / neuroprotection

Sponsor
Neurotech Pharmaceuticals
Treatment
NT-501; NT-501
Gene
Not stated
Conditions
Retinitis Pigmentosa
Ages
18 Years to 64 Years
Enrollment
73 participants
Started
2007-01-22
Main results expected
2010-04-19
Results posted
Yes
Record last updated
2025-05-01

What the study is testing

The purpose of this study is to look at the safety and effectiveness of CNTF implants on vision in persons with retinitis pigmentosa, Usher type II \& III, and Choroideremia. This research is being done because there are no effective therapies for people with these retinal degenerations. They are genetic disorders that affect one's ability to see at night, and later cause tunnel vision and loss of central vision. Retinal degenerations affect the retina, a light sensitive layer of cells in the back of the eye. Slowly over time, these cells die and cause permanent loss of vision.

The implant is a small capsule that contains human retinal pigment epithelium cells. These cells have been given the ability to make CNTF and release it through the capsule membrane into the surrounding fluid. In this study, two different CNTF dose levels will be used: a high dose and a low dose in one eye, as well as a sham (or placebo) surgery in the other eye.

Where it runs

United States (12)

Open on ClinicalTrials.gov for contacts and eligibility